KMID : 0624620230560040252
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BMB Reports 2023 Volume.56 No. 4 p.252 ~ p.257
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Determination of HIF-1¥á degradation pathways via modulation of the propionyl mark
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Jeong Kwan-Young
Choi Jin-Mi Choi Ah-Rum Shim Joo-Hee Kim Young-Ah Oh Chang-Seok Youn Hong-Duk Cho Eun-Jung
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Abstract
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The hypoxia-inducible factor-1¥á (HIF-1¥á) is a key regulator of hypoxic stress under physiological and pathological conditions. HIF-1¥á protein stability is tightly regulated by the ubiquitin-proteasome system (UPS) and autophagy in normoxia, hypoxia, and the tumor environment to mediate the hypoxic response. However, the mechanisms of how the UPS and autophagy interplay for HIF-1¥á proteostasis remain unclear. Here, we found a HIF-1¥á species propionylated at lysine (K) 709 by p300/CREB binding protein (CBP). HIF-1¥á stability and the choice of degradation pathway were affected by HIF-1¥á propionylation. K709-propionylation prevented HIF-1¥á from degradation through the UPS, while activated chaperon-mediated autophagy (CMA) induced the degradation of propionylated and nonpropionylated HIF-1¥á. CMA contributed to HIF-1¥á degradation in both normoxia and hypoxia. Furthermore, the pan-cancer analysis showed that CMA had a significant positive correlation with the hypoxic signatures, whereas SIRT1, responsible for K709-depropionylation correlated negatively with them. Altogether, our results revealed a novel mechanism of HIF-1¥á distribution into two different degradation pathways.
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KEYWORD
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Chaperone-mediated autophagy, HIF-1¥á, p300, SIRT1, Ubiquitin-proteasome system
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